Tcf4 Controls Neuronal Migration of the Cerebral Cortex through Regulation of Bmp7

por Chen, Tianda, Wu, Qinwei, Zhang, Yang, Lu, Tianlan, Yue, Weihua, Zhang, Dai
Publicado 2016

C677T Polymorphism in the MTHFR Gene Is Associated With Risperidone-Induced Weight Gain in Schizophrenia

por Liao, Jingping, Wang, Ning, Ma, Mengying, Lu, Tianlan, Yan, Hao, Yue, Weihua
Publicado 2020

Association of MTHFR C677T Polymorphism With Antipsychotic-Induced Change of Weight and Metabolism Index

por Su, Yi, Yan, Hao, Guo, Liangkun, Lu, Tianlan, Zhang, Dai, Yue, Weihua
Publicado 2021

RAB18, a protein associated with Warburg Micro syndrome, controls neuronal migration in the developing cerebral cortex

por Wu, Qinwei, Sun, Xiaqin, Yue, Weihua, Lu, Tianlan, Ruan, Yanyan, Chen, Tianda, Zhang, Dai
Publicado 2016

Growth arrest specific gene 7 is associated with schizophrenia and regulates neuronal migration and morphogenesis

por Zhang, Zhengrong, Zheng, Fanfan, You, Yang, Ma, Yuanlin, Lu, Tianlan, Yue, Weihua, Zhang, Dai
Publicado 2016

Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia

por Liang, Wei, Yu, Hao, Su, Yi, Lu, Tianlan, Yan, Hao, Yue, Weihua, Zhang, Dai
Publicado 2020

CYP2D6 Genotype-Based Dose Recommendations for Risperidone in Asian People

por Cui, Yuanxia, Yan, Hao, Su, Yi, Wang, Lifang, Lu, Tianlan, Zhang, Dai, Yue, Weihua
Publicado 2020

Autism spectrum disorder research: knowledge mapping of progress and focus between 2011 and 2022

por Jiang, Miaomiao, Lu, Tianlan, Yang, Kang, Li, Xianjing, Zhao, Liyang, Zhang, Dai, Li, Jun, Wang, Lifang
Publicado 2023

Comparison of the probability of four anticonvulsant mood stabilizers to facilitate polycystic ovary syndrome in women with epilepsies or bipolar disorder—A systematic review and m...

por Guo, Jing, Liu, Yan, Kong, Lingling, Sun, Yaoyao, Lu, Zhe, Lu, Tianlan, Qu, Haiying, Yue, Weihua
Publicado 2023

Genome-wide association study identified six loci associated with adverse drug reactions to aripiprazole in schizophrenia patients

por Wang, Xueping, Mei, Dongli, Lu, Zhe, Zhang, Yuyanan, Sun, Yaoyao, Lu, Tianlan, Yan, Hao, Yue, Weihua
Publicado 2023

Phosphodiesterase and psychiatric disorders: a two-sample Mendelian randomization study

por Jiang, Miaomiao, Yan, Weiheng, Zhang, Yuyanan, Lu, Zhe, Lu, Tianlan, Zhang, Dai, Li, Jun, Wang, Lifang
Publicado 2023

Calcium Homeostasis and Psychiatric Disorders: A Mendelian Randomization Study

por Jiang, Miaomiao, Yan, Weiheng, Li, Xianjing, Zhao, Liyang, Lu, Tianlan, Zhang, Dai, Li, Jun, Wang, Lifang
Publicado 2023

Replication of Association between Schizophrenia and Chromosome 6p21-6p22.1 Polymorphisms in Chinese Han Population

por Zhang, Yang, Lu, Tianlan, Yan, Hao, Ruan, Yanyan, Wang, Lifang, Zhang, Dai, Yue, Weihua, Lu, Lin
Publicado 2013

Evidence for Association of Cell Adhesion Molecules Pathway and NLGN1 Polymorphisms with Schizophrenia in Chinese Han Population

por Zhang, Zhengrong, Yu, Hao, Jiang, Sisi, Liao, Jinmin, Lu, Tianlan, Wang, Lifang, Zhang, Dai, Yue, Weihua
Publicado 2015

Genome-wide DNA methylation analysis in obsessive-compulsive disorder patients

por Yue, Weihua, Cheng, Weiqiu, Liu, Zhaorui, Tang, Yi, Lu, Tianlan, Zhang, Dai, Tang, Muni, Huang, Yueqin
Publicado 2016

Cerebral Inefficient Activation in Schizophrenia Patients and Their Unaffected Parents during the N-Back Working Memory Task: A Family fMRI Study

por Jiang, Sisi, Yan, Hao, Chen, Qiang, Tian, Lin, Lu, Tianlan, Tan, Hao-Yang, Yan, Jun, Zhang, Dai
Publicado 2015

A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population

por Yue, Weihua, Yang, Yongfeng, Zhang, Yanling, Lu, Tianlan, Hu, Xiaofeng, Wang, Lifang, Ruan, Yanyan, Lv, Luxian, Zhang, Dai
Publicado 2011

Evidence for association between Disrupted-in-schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study

por Zheng, Fanfan, Wang, Lifang, Jia, Meixiang, Yue, Weihua, Ruan, Yan, Lu, Tianlan, Liu, Jing, Li, Jun, Zhang, Dai
Publicado 2011

Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia

por Ma, Yuanlin, Li, Jun, Yu, Hao, Wang, Lifang, Lu, Tianlan, Pan, Chao, Han, Yonghua, Zhang, Dai, Yue, Weihua
Publicado 2015

Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population

por Wang, Ziqi, Zhang, Tian, Liu, Jing, Wang, Han, Lu, Tianlan, Jia, Meixiang, Zhang, Dai, Wang, Lifang, Li, Jun
Publicado 2019